论文标题
固定剂对用RP-CARS显微镜探测的髓磷脂分子顺序的影响
Effects of fixatives on myelin molecular order probed with RP-CARS microscopy
论文作者
论文摘要
当实时成像不可行时,样品固定允许保留生物样品的超微结构以进行随后的显微镜分析。可以使用各种方法进行此过程,每种方法都会影响样品的生物结构。尽管这些改变是使用传统显微镜进行了充分特征的,但几乎没有有关固定剂对生物组织空间分子方向的影响的信息。我们通过采用旋转偏振相干的抗螺旋式拉曼散射(RP-CARS)显微镜来研究不同固定剂对髓磷脂亚微米分子级和显微标准形态的影响,从而解决了这一问题。 RP-CARS是一种源自汽车显微镜的新技术,它允许探测分子键的空间取向,同时保持汽车显微镜的内在化学选择性。通过表征固定程序的效果,目前的工作代表了选择最佳固定技术的有用指南,尤其是极化分辨的汽车显微镜。最后,我们表明,只要考虑到对分子空间分布的影响(此处表征),可以有效利用多聚甲醛和戊二醛作为RP-CARS显微镜的固定剂的组合。
When live imaging is not feasible, sample fixation allows preserving the ultrastructure of biological samples for subsequent microscopy analysis. This process could be performed with various methods, each one affecting differently the biological structure of the sample. While these alterations were well-characterized using traditional microscopy, little information is available about the effects of the fixatives on the spatial molecular orientation of the biological tissue. We tackled this issue by employing Rotating-Polarization Coherent Anti-Stokes Raman Scattering (RP-CARS) microscopy to study the effects of different fixatives on the myelin sub-micrometric molecular order and micrometric morphology. RP-CARS is a novel technique derived from CARS microscopy that allows probing spatial orientation of molecular bonds while maintaining the intrinsic chemical selectivity of CARS microscopy. By characterizing the effects of the fixation procedures, the present work represents a useful guide for the choice of the best fixation technique(s), in particular for polarisation-resolved CARS microscopy. Finally, we show that the combination of paraformaldehyde and glutaraldehyde can be effectively employed as a fixative for RP-CARS microscopy, as long as the effects on the molecular spatial distribution, here characterized, are taken into account.